Literature DB >> 33367737

Brain cell type-specific endocytosis of arylsulfatase A identifies limitations of enzyme-based therapies for metachromatic leukodystrophy.

Debora Kaminski, Claudia Yaghootfam, Frank Matthes, Annika Reßing, Volkmar Gieselmann, Ulrich Matzner.   

Abstract

Enzyme replacement therapies, allogeneic bone marrow transplantation and gene therapies are treatment options for lysosomal storage diseases caused by inherited deficiencies of soluble lysosomal enzymes. Independent from the approach, the enzyme must be delivered to lysosomes of deficient patient cells. Little is known about the dissemination of enzyme within a tissue where cells compete for uptake via different receptor systems, binding affinities and endocytic rates. To evaluate dissemination and lysosomal targeting of a lysosomal enzyme in the CNS, we analysed receptor-mediated endocytosis of arylsulfatase A (ASA) by different types of brain-derived cell lines and primary murine brain cells. For ASA expressed by chinese hamster ovary cells for enzyme replacement therapy of metachromatic leukodystrophy, endocytic rates decline from microglia to neurons and astrocytes and to oligodendrocytes. Only immature oligodendrocytes endocytose significant amounts of enzyme. Uptake by non-microglial cells is due to mannose 6-phosphate receptors, whereas several receptor systems participate in endocytosis by microglial cells. Interestingly, ASA expressed by microglial cells cannot be taken up in a mannose 6-phosphate dependent manner. The resulting failure to correct non-microglial cells corroborates in vivo data and indicates that therapeutic effects of allogeneic bone marrow transplantation and hematopoietic stem cell gene therapy on metachromatic leukodystrophy are independent of metabolic cross-correction of neurons, astrocytes and oligodendrocytes by receptor-mediated endocytosis.
© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Year:  2021        PMID: 33367737     DOI: 10.1093/hmg/ddaa277

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  6 in total

1.  New disease modifying therapies for two genetic childhood-onset neurometabolic disorders (metachromatic leucodystrophy and adrenoleucodystrophy).

Authors:  Antonio Federico; Marianne de Visser
Journal:  Neurol Sci       Date:  2021-07-01       Impact factor: 3.307

2.  Neurofilament light chain and glial fibrillary acidic protein levels in metachromatic leukodystrophy.

Authors:  Shanice Beerepoot; Hans Heijst; Birthe Roos; Mirjam M C Wamelink; Jaap Jan Boelens; Caroline A Lindemans; Peter M van Hasselt; Edwin H Jacobs; Marjo S van der Knaap; Charlotte E Teunissen; Nicole I Wolf
Journal:  Brain       Date:  2022-03-29       Impact factor: 15.255

Review 3.  Emerging cellular themes in leukodystrophies.

Authors:  Joseph C Nowacki; Ashley M Fields; Meng Meng Fu
Journal:  Front Cell Dev Biol       Date:  2022-08-08

Review 4.  Mucopolysaccharidoses and the blood-brain barrier.

Authors:  Onur Sahin; Hannah P Thompson; Grant W Goodman; Jun Li; Akihiko Urayama
Journal:  Fluids Barriers CNS       Date:  2022-09-19

5.  Efficacy and Safety of a Krabbe Disease Gene Therapy.

Authors:  Juliette Hordeaux; Brianne A Jeffrey; Jinlong Jian; Gourav R Choudhury; Kristofer Michalson; Thomas W Mitchell; Elizabeth L Buza; Jessica Chichester; Cecilia Dyer; Jessica Bagel; Charles H Vite; Allison M Bradbury; James M Wilson
Journal:  Hum Gene Ther       Date:  2022-03-22       Impact factor: 4.793

6.  Expression of Ripk1 and DAM genes correlates with severity and progression of Krabbe disease.

Authors:  María B Cachón-González; Susan Wang; Timothy M Cox
Journal:  Hum Mol Genet       Date:  2021-11-01       Impact factor: 6.150

  6 in total

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